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Table 5 Medical consultation 40 to 56 days after boost COVID-19 vaccination separated by gender

From: Reactogenicity after heterologous and homologous COVID-19 prime-boost vaccination regimens: descriptive interim results of a comparative observational cohort study

  

Female

  

Male

 
 

ChAdOx1/ ChAdOx1

ChAdOx1/ mRNA

mRNA/ mRNA

ChAdOx1/ ChAdOx1

ChAdOx1/ mRNA

mRNA/ mRNA

 

(n = 205)

(n = 1189)

(n = 2865)

(n = 257)

(n = 448)

(n = 2133)

Medical consultation, thereof...

33 (16.1%)

233 (19.6%)

533 (18.6%)

36 (14%)

53 (11.8%)

261 (12.2%)

Outpatient

      

Yes

32 (97.0%)

205 (88.0%)

453 (85.0%)

29 (80.6%)

42 (79.2%)

213 (81.6%)

Planned

1 (3.0%)

27 (11.6%)

75 (14.1%)

5 (13.9%)

9 (17.0%)

41 (15.7%)

No

0 (0%)

1 (0.4%)

5 (0.9%)

2 (5.6%)

2 (3.8%)

7 (2.7%)

Inpatient/Clinic

      

Yes

5 (15.2%)

16 (6.9%)

44 (8.3%)

8 (22.2%)

5 (9.4%)

41 (15.7%)

Planned

0 (0%)

2 (0.9%)

5 (0.9%)

1 (2.8%)

0 (0%)

4 (1.5%)

No

28 (84.8%)

215 (92.3%)

484 (90.8%)

27 (75.0%)

48 (90.6%)

216 (82.8%)

Pre-existing conditions

   

Yes

2 (6.1%)

28 (12.0%)

60 (11.3%)

9 (25.0%)

12 (22.6%)

43 (16.5%)

Partially

10 (30.3%)

85 (36.5%)

217 (40.7%)

12 (33.3%)

10 (18.9%)

73 (28.0%)

No

21 (63.6%)

120 (51.5%)

256 (48%)

15 (41.7%)

31 (58.5%)

145 (55.6%)

Suspected association to vaccination

   

Yes

1 (3%)

16 (6.9%)

26 (4.9%)

2 (5.6%)

0 (0%)

10 (3.8%)

Partially

4 (12.1%)

49 (21%)

118 (22.1%)

6 (16.7%)

11 (20.8%)

53 (20.3%)

No

28 (84.8%)

168 (72.1%)

389 (73%)

28 (77.8%)

42 (79.2%)

198 (75.9%)

  1. Health problems reported in the long-term survey 40 to 56 days after boost COVID-19 vaccination with ChAdOx1 or mRNA vaccine in cohorts of participants with homologous (mRNA/mRNA or ChAdOx1/ChAdOx1) or heterologous (ChAdOx1/mRNA) prime-boost COVID-19 vaccination regimen who completed the long-term survey. ChAdOx1: ChAdOx1 (AstraZeneca). mRNA: BNT162b2 (BioNTech/Pfizer) or mRNA-1273 (Moderna)